Variant report

Variant rs719162
Chromosome Location chr8:52311584-52311585
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:52307000-52312400 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
2 chr8:52307600-52320600 Weak transcription Right Ventricle heart
3 chr8:52308600-52317800 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
4 chr8:52309000-52312400 Weak transcription Gastric stomach
5 chr8:52309000-52318200 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
6 chr8:52309000-52319000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
7 chr8:52309400-52316000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr8:52310200-52312400 Enhancers NH-A brain
9 chr8:52310400-52312200 Enhancers NHDF-Ad bronchial
10 chr8:52310400-52312400 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
11 chr8:52310600-52312200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
12 chr8:52310600-52312400 Enhancers Osteobl bone
13 chr8:52310800-52311600 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr8:52310800-52311600 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
15 chr8:52310800-52311800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
16 chr8:52311000-52317200 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
17 chr8:52311000-52321200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
18 chr8:52311200-52318400 Weak transcription Left Ventricle heart
19 chr8:52311400-52312800 Weak transcription Primary B cells from peripheral blood blood

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